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Ipratropium bromide
Ipratropium bromide - 24208-398-30 - (Ipratropium bromide)
Drug Information of Ipratropium bromide
| Product NDC: | 24208-398 |
| Proprietary Name: | Ipratropium bromide |
| Non Proprietary Name: | Ipratropium bromide |
| Active Ingredient(s): | 21 ug/1 & nbsp; Ipratropium bromide |
| Administration Route(s): | NASAL |
| Dosage Form(s): | SPRAY, METERED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ipratropium bromide
| Product NDC: | 24208-398 |
| Labeler Name: | Bausch & Lomb Incorporated |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076025 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20030331 |
Package Information of Ipratropium bromide
| Package NDC: | 24208-398-30 |
| Package Description: | 1 BOTTLE, SPRAY in 1 CARTON (24208-398-30) > 345 SPRAY, METERED in 1 BOTTLE, SPRAY |
NDC Information of Ipratropium bromide
| NDC Code | 24208-398-30 |
| Proprietary Name | Ipratropium bromide |
| Package Description | 1 BOTTLE, SPRAY in 1 CARTON (24208-398-30) > 345 SPRAY, METERED in 1 BOTTLE, SPRAY |
| Product NDC | 24208-398 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ipratropium bromide |
| Dosage Form Name | SPRAY, METERED |
| Route Name | NASAL |
| Start Marketing Date | 20030331 |
| Marketing Category Name | ANDA |
| Labeler Name | Bausch & Lomb Incorporated |
| Substance Name | IPRATROPIUM BROMIDE |
| Strength Number | 21 |
| Strength Unit | ug/1 |
| Pharmaceutical Classes | Anticholinergic [EPC],Cholinergic Antagonists [MoA] |
